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Study identifier: NCT04874350 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

A Study to Assess the Efficacy, Safety, and Tolerability of Oral LPCN 1148 in Male Subjects With Cirrhosis of the Liver and Sarcopenia

Condition: Liver Cirrhosis · Sarcopenia  ·  Sponsor: Lipocine Inc.

PhasePhase 2
Planned participants30
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a randomized, double-blind, placebo-controlled study to assess the efficacy, safety, and tolerability of LPCN 1148 in men with cirrhosis of the liver and sarcopenia.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (10)

Mayo ClinicScottsdale, Arizona, United States
University of California, Los AngelesLos Angeles, California, United States
University of California San FranciscoSan Francisco, California, United States
University of Maryland Medical CenterBaltimore, Maryland, United States
Beth Israel Deaconess Medical CenterBoston, Massachusetts, United States
Methodist Health SystemDallas, Texas, United States
University of Texas SouthwesternDallas, Texas, United States
Mt.Olympus Medical ResearchHouston, Texas, United States
Intermountain HealthcareMurray, Utah, United States
University of UtahSalt Lake City, Utah, United States

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Source record: clinicaltrials.gov/study/NCT04874350